Jamaicamide A Explained

Jamaicamide A is a lipopeptide isolated from the cyanobacterium Moorea producens, formerly known as Lyngbya majuscula.[1] Jamaicamide A belongs to a family of compounds collectively called jamaicamides, which are sodium channel blockers with potent neurotoxicity in a cellular model. Jamaicamide A has several unusual functionalities, including an alkynyl bromide, vinyl chloride, β-methoxy eneone system, and pyrrolinone ring.

History

Jamaicamide A was discovered by William H. Gerwick from Oregon State University, Corvallis, Oregon, USA. This natural product was isolated from a dark green strain of Moorea producens, formerly known as Lyngbya majuscula, marine cyanobacteria collected from Hector Bay, Jamaica. The initial small amount of crude extract has shown potent brine shrimp toxicity. The organism was cultured in the laboratory, producing ten g/l of biomass after six weeks. The compound was extracted using standard methods for lipid natural products, and the fractionation process was performed using vacuum liquid chromatography (VLC).[2]

Jamaicamide A exhibited moderate in vitro cytotoxicity to H-460 human lung and Neuro-2a mouse neuroblastoma cell lines with an IC50 value of 15 μM for both cell lines. This compound also displayed low micromolar inhibition of sodium channel-blocking activity at 5 μM. In a goldfish toxicity assay, compared with other Jamaicamides such as Jamaicamide B and C, Jamaicamide A has the least active fish toxin (sublethal toxicity at 10 ppm after 90 min), and neither showed significant brine shrimp toxicity.[2]

Biosynthesis

It has been predicted that jamaicamide A's biosynthetic pathways are from a hybrid polyketide synthase-nonribosomal peptide synthetase (PKS-NRPS) assembly units. Jamaicamide A is a popetides with a colinear arrangement with a chemical structure that suggests it is derived from various polyketides (9 acetate units), amino acids (L-Ala and β-Ala), and methionine-derived methyl groups. Nevertheless, it has distinctive molecular features like the terminal alkynyl bromide, vinyl chloride, and pyrrolinone ring. The biosynthetic origins and mechanism of formation of the pyrrolinone ring system are unknown.[2]

The first proposed biosynthesis of jamaicamide A published in 2004.[2] Another proposed biosynthesis of jamaicamide A was published in 2006.[3]

Notes and References

  1. Ma . Liang . Zhang . Qingbo . Yang . Chunfang . Zhu . Yiguang . Zhang . Liping . Wang . Lijuan . Liu . Zhiwen . Zhang . Guangtao . Zhang . Changsheng . 1.06 - Assembly Line and Post-PKS Modifications in the Biosynthesis of Marine Polyketide Natural Products . Comprehensive Natural Products III . 2020. 139–197 . 10.1016/B978-0-12-409547-2.14711-0 . 9780081026915 . 213115096 . 20 May 2023.
  2. Edwards . Daniel J. . Marquez . Brian L. . Nogle . Lisa M. . McPhail . Kerry . Goeger . Douglas E. . Roberts . Mary Ann . Gerwick . William H. . Structure and Biosynthesis of the Jamaicamides, New Mixed Polyketide-Peptide Neurotoxins from the Marine Cyanobacterium Lyngbya majuscula . Chemistry & Biology . 2004 . 11 . 6 . 817–833 . 10.1016/j.chembiol.2004.03.030 . 15217615 . free .
  3. Vaillancourt . Frédéric H. . Yeh . Ellen . Vosburg . David A. . Garneau-Tsodikova . Sylvie . Walsh . Christopher T. . Nature's Inventory of Halogenation Catalysts: Oxidative Strategies Predominate . Chemical Reviews . 2006 . 106 . 8 . 3364–3378 . 10.1021/cr050313i . 16895332 .